Trials / Completed
CompletedNCT02213159
Dexmedetomidine for Postoperative Analgesia After Bariatric Surgery
Intraoperative Dexmedetomidine Versus Morphine for Postoperative Analgesia After Laparoscopic Bariatric Surgery
- Status
- Completed
- Phase
- Phase 2 / Phase 3
- Study type
- Interventional
- Enrollment
- 60 (actual)
- Sponsor
- American University of Beirut Medical Center · Academic / Other
- Sex
- All
- Age
- 18 Years – 70 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to determine if Dexmedetomidine given at the end of surgery will reduce postoperative morphine consumption and improve postoperative quality of recovery as compared to morphine in patients undergoing laparoscopic bariatric surgery.
Detailed description
effect of Dexmedetomidine bolus on postoperative morphine requirements
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Dexmedetomidine | |
| DRUG | Morphine |
Timeline
- Start date
- 2014-07-01
- Primary completion
- 2015-11-01
- Completion
- 2015-12-01
- First posted
- 2014-08-11
- Last updated
- 2016-07-13
Locations
1 site across 1 country: Lebanon
Source: ClinicalTrials.gov record NCT02213159. Inclusion in this directory is not an endorsement.